Healthy Clinical Trial
Official title:
A Phase 1 Clinical Trial to Evaluate the Effect of Food on the Pharmacokinetics and Safety of DWP16001 After Administration in Healthy Adult Volunteers
This study aims to evaluate the effect of food on the pharmacokinetics and safety of DWP16001 after oral administration.
Status | Recruiting |
Enrollment | 32 |
Est. completion date | November 30, 2023 |
Est. primary completion date | May 31, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 19 Years and older |
Eligibility | Inclusion Criteria: 1. A person who has decided to participate voluntarily and agreed in writing prior to the screening procedure after understanding the detailed explanation of this clinical trial. 2. A person who is 19 years of age or more at the time of screening. 3. Those with a weight of 50.0 kg or more and a body mass index (BMI) of 18.0 kg/m2 or more and 30.0 kg/m2 or less. Exclusion Criteria: 1. A person who has a genetic problem such as galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption. 2. A person who has a history of gastrointestinal surgery/disease, such as Crohn's disease, ulcer, acute or chronic pancreatitis, which may affect the absorption of drug for clinical trials. (Except for simple appendectomy or hernia surgery) |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Chungbuk National University Hospital | Chungbuk |
Lead Sponsor | Collaborator |
---|---|
Daewoong Pharmaceutical Co. LTD. |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | AUC0-t of DWP16001 | AUC0-t of DWP16001 | 0 to 72 hours | |
Primary | Cmax of DWP16001 | Cmax of DWP16001 | 0 to 72 hours |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
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